Medical Oncology Department, University Hospital Miguel Servet, Av. Isabel la Católica 1-3, 50009, Zaragoza, Spain.
Radiation Oncology Service, Institut Català D'Oncologia (ICO) Hospitalet, Barcelona, Spain.
Clin Transl Oncol. 2021 Aug;23(8):1666-1677. doi: 10.1007/s12094-021-02567-z. Epub 2021 Apr 19.
Sequential treatment of Panitumumab (Pb) plus Paclitaxel (Px) as induction treatment (IT) followed by concurrent bioradiotherapy (Bio-RT) with Pb may be an alternative for locally advanced squamous cell carcinoma of the head and neck (LA-SCCHN) in patients ineligible for high-dose cisplatin therapy.
Phase II, single-arm, multicentre study, with two-stage design, in patients ≥ 18 years with stage III-IVa-b LA-SCCHN unfit for platinum. Patients received Px + Pb (9 weeks) as IT followed by Bio-RT + Pb. Primary endpoint: overall response rate (ORR) after IT, defined as: more than 70% of patients achieving complete response (CR) or partial response (PR) to IT. Secondary end-points: progression-free survival, organ preservation rate, safety profile.
Study ended prematurely (51 patients) due to slow recruitment. ORR: 66.7% (95% CI: 53.7-79.6), 8 (15.7%) CR and 26 (51.0%) PR. 39 patients (76%) completed radiotherapy (RT). Pb and/or Px-related adverse events (AEs) grade 3-4: 56.9% during IT and 63.4% during the concomitant phase, of which most common were skin toxicity (33.3%). Five deaths occurred during treatment, two of them (3.9%) were Pb and/or Px-related.
Although underpowered, ORR was higher than the pre-specified boundary for considering the treatment active. Although Px + Pb as IT provides some benefit, the safety profile is worse than expected. To consider Pb + Px as IT as an alternative for platinum-unsuitable LA-SCCHN, further research/investigation would be needed.
帕尼单抗(Pb)联合紫杉醇(Px)序贯治疗(IT)作为诱导治疗(IT),随后联合生物放疗(Bio-RT)和帕尼单抗(Pb)可能是不适合大剂量顺铂治疗的局部晚期头颈部鳞状细胞癌(LA-SCCHN)患者的另一种选择。
这是一项 II 期、单臂、多中心研究,采用两阶段设计,纳入年龄≥18 岁、不适合铂类药物的 III-IVa-b 期 LA-SCCHN 患者。患者接受 Px+Pb(9 周)作为 IT,随后进行 Bio-RT+Pb。主要终点:IT 后的总缓解率(ORR),定义为:超过 70%的患者对 IT 有完全缓解(CR)或部分缓解(PR)。次要终点:无进展生存期、器官保存率、安全性。
由于招募缓慢,研究提前结束(51 例)。ORR:66.7%(95%CI:53.7-79.6),8 例(15.7%)CR 和 26 例(51.0%)PR。39 例(76%)患者完成了放疗(RT)。在 IT 期间和同时期,与 Pb 和/或 Px 相关的 3-4 级不良事件(AE)分别为 56.9%和 63.4%,其中最常见的是皮肤毒性(33.3%)。治疗期间发生 5 例死亡,其中 2 例(3.9%)与 Pb 和/或 Px 相关。
尽管效力不足,但 ORR 高于考虑治疗有效的预定界限。虽然 Pb+Px 作为 IT 提供了一些益处,但安全性不如预期。为了考虑 Pb+Px 作为不适合铂类药物的 LA-SCCHN 的 IT 替代方案,需要进一步的研究/调查。